38660-83-2

Upstream product

• 68230-35-3 3-Methyl-2-phenyl-2-phenylamino-butyronitrile 
• 62-53-3 aniline 
• 611-70-1 phenyl isopropyl ketone 
• 37951-09-0 2-methyl-1,1-diphenyl-propan-1-ol 

Downstream Products

• 38425-87-5 4,4-Dimethyl-5-phenyl-5-phenylimino-valeronitril 
• 145909-49-5 α-(1-methylethyl)-N-phenyl-benzenemethanamine 
• 134590-22-0 N-Phenyl-N-(2-chloro-2-methyl-1-phenyl)-1-propylamine 
• 106700-36-1 2-Chloro-N-(2-methyl-1-phenyl-propenyl)-N-phenyl-acetamide 
• 68230-42-2 N-(1-phenyl-2-methylpropyl)-aniline 
• 137208-26-5 [2-Bromo-2-methyl-1-phenyl-prop-(E)-ylidene]-phenyl-amine 
• 134590-21-9 N-(2-chloro-2-methyl-1-phenyl-1-propylidene)aniline 

Relevant academic research and scientific papers

Iodine-mediated 1,2-aryl migration of primary benzhydryl amines

An iodine-mediated 1,2-aryl migration reaction of primary benzhydryl amines under transition metal-free conditions has been achieved. The crude imines generated by this rearrangement reaction can be directly transformed into various aromatic secondary ami

Iron-catalysed 1,2-aryl migration of tertiary azides

1,2-Aryl migration of α,α-diaryl tertiary azides was achieved by using the catalytic system of FeCl2/N-heterocyclic carbene (NHC) SIPr·HCl. The reaction generated aniline products in good yields after one-pot reduction of the migration-resultant imines.

Development of highly enantioselective new Lewis basic N-formamide organocatalysts for hydrosilylation of imines with an unprecedented substrate profile

l-Pipecolinic acid derived N-formamides have been developed as new Lewis basic organocatalysts that promote the asymmetric reduction of N-aryl ketimines using trichlorosilane as the reducing agent. The substituent on N4 of the piperazinyl backbone and the

Synthesis and Herbicidal Activity of N-(1-Arylethenyl)-2-chloroacetamides

N-(1-Alkenyl)-2-chloroacetamides, which bear an aryl substituent at the 1-position of the alkenyl moiety, were synthesized and their herbicidal activities were tested.Some of them were active against paddy field weeds.In particular, a new type of chloroac

Asymmetric Reduction of Schiff's Bases with Lithium Aluminium Hydride-Monosaccharide Complexes to Give Optically Active Secondary Amines

The asymmetric reduction of selected Schiff's bases (ketimines) with the lithium aluminium hydride-monosaccharide complexes derived from 3-O-benzyl-1,2-O-cyclohexylidene-α-D-glucofuranose gives optically active secondary amines.The absolute configuration